1,2-Dichloroethane → HCID 68429731、化合物

HRID 335614ノート

反応式

HRID 335614 の反応式
[N+:1]([C:4]1[C:12]2[S:11][C:10]([C:13]([OH:15])=O)=[CH:9][C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:16](Cl)[CH2:17][Cl:18].[CH:20]1[CH:21]=C[C:23]2[N:28](O)N=[N:26][C:24]=2[CH:25]=1.C(N(CC)CC)C>CN(C=O)C>[ClH:18].[N:28]12[CH2:17][CH2:16][CH:25]([CH2:20][CH2:21]1)[C@@H:24]([NH:26][C:13]([C:10]1[S:11][C:12]3[C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=[CH:7][C:8]=3[CH:9]=1)=[O:15])[CH2:23]2

参加物

6

反応物 4

HCID 111,2-DichloroethaneHCID 8471TriethylamineHCID 757711-HydroxybenzotriazoleHCID 131624097-Nitrobenzo[b]thiophene-2-carboxylic acid

生成物 1

HCID 68429731HCID 68429731、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2.0 g (8.96 mmol) of 7-nitro-1-benzothiophene-2-carboxylic acid and 1.78 g (8.96 mmol) of R-3-aminoquinuclidine dihydrochloride are initially charged in 25 ml of DMF. At 0° C., 2.06 g (10.75 mmol) of EDC, 1.45 g (10.75 mmol) of HOBt and 4.50 ml (32.26 mmol) of triethylamine are added to the solution. The mixture is stirred at RT for 18 h. The reaction is terminated by addition of a 10% strength aqueous sodium bicarbonate solution, and ethyl acetate is added. The resulting precipitate is filtered off with suction. The mother liquor is extracted twice with ethyl acetate. The organic phases are combined and concentrated. Both the precipitate and the concentrated mother liquor are purified by silica gel column chromatography (mobile phase: dichloromethane/methanol/25% ammonia 100:10:2). The product fractions are concentrated, dissolved in a mixture of methanol and 1N hydrochloric acid, then again concentrated and dried under high vacuum. The resulting solid is triturated with acetonitrile, filtered off with suction and dried at 50° C. under reduced pressure. 1.10 g (32.8% of theory) of the title compound are obtained.

後処理

  1. customThe reaction is terminated by addition of a 10% strength aqueous sodium bicarbonate solution, and ethyl acetate
  2. additionis added
  3. filtrationThe resulting precipitate is filtered off with suction
  4. extractionThe mother liquor is extracted twice with ethyl acetate
  5. concentrationconcentrated
  6. customBoth the precipitate and the concentrated mother liquor are purified by silica gel column chromatography (mobile phase: dichloromethane/methanol/25% ammonia 100:10:2)
  7. concentrationThe product fractions are concentrated
  8. dissolutiondissolved in a mixture of methanol and 1N hydrochloric acid
  9. concentrationagain concentrated
  10. customdried under high vacuum
  11. customThe resulting solid is triturated with acetonitrile
  12. filtrationfiltered off with suction
  13. customdried at 50° C. under reduced pressure

出典と根拠

ORDレコード
ord-e84c934630c14cbb923569db7456b88c
出典データセット
uspto-grants-2014_11
特許番号
US08884017B2

反応ノート

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